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	1.	A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disorders. [electronic resource] by Swanson, D A Freund, C L Ploder, L McInnes, R R Valle, D Producer: 19961024 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Pax-6, Prox 1, and Chx10 homeobox gene expression correlates with phenotypic fate of retinal precursor cells. [electronic resource] by Belecky-Adams, T Tomarev, S Li, H S Ploder, L McInnes, R R Sundin, O Adler, R Producer: 19970626 In: Investigative ophthalmology & visual science vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	3.	Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cells. [electronic resource] by Chow, R L Snow, B Novak, J Looser, J Freund, C Vidgen, D Ploder, L McInnes, R R Producer: 20020321 In: Mechanisms of development vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A differential hybridization scheme to identify photoreceptor-specific genes. [electronic resource] by Swanson, D A Freund, C L Steel, J M Xu, S Ploder, L McInnes, R R Valle, D Producer: 19970804 In: Genome research vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Intragenic complementation at the human argininosuccinate lyase locus. Identification of the major complementing alleles. [electronic resource] by Walker, D C Christodoulou, J Craig, H J Simard, L R Ploder, L Howell, P L McInnes, R R Producer: 19970414 In: The Journal of biological chemistry vol. 272 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Developmental expression of a novel murine homeobox gene (Chx10): evidence for roles in determination of the neuroretina and inner nuclear layer. [electronic resource] by Liu, I S Chen, J D Ploder, L Vidgen, D van der Kooy, D Kalnins, V I McInnes, R R Producer: 19940922 In: Neuron vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Intragenic complementation at the argininosuccinate lyase locus: reconstruction of the active site. [electronic resource] by Howell, P L Turner, M A Christodoulou, J Walker, D C Craig, H J Simard, L R Ploder, L McInnes, R R Producer: 19981008 In: Journal of inherited metabolic disease vol. 21 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	PHR1 encodes an abundant, pleckstrin homology domain-containing integral membrane protein in the photoreceptor outer segments. [electronic resource] by Xu, S Ladak, R Swanson, D A Soltyk, A Sun, H Ploder, L Vidgen, D Duncan, A M Garami, E Valle, D McInnes, R R Producer: 20000113 In: The Journal of biological chemistry vol. 274 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis. [electronic resource] by Clarke, G Goldberg, A F Vidgen, D Collins, L Ploder, L Schwarz, L Molday, L L Rossant, J Szél, A Molday, R S Birch, D G McInnes, R R Producer: 20000612 In: Nature genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation. [electronic resource] by Burmeister, M Novak, J Liang, M Y Basu, S Ploder, L Hawes, N L Vidgen, D Hoover, F Goldman, D Kalnins, V I Roderick, T H Taylor, B A Hankin, M H McInnes, R R Producer: 19960703 In: Nature genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. [electronic resource] by Ferda Percin, E Ploder, L A Yu, J J Arici, K Horsford, D J Rutherford, A Bapat, B Cox, D W Duncan, A M Kalnins, V I Kocak-Altintas, A Sowden, J C Traboulsi, E Sarfarazi, M McInnes, R R Producer: 20000828 In: Nature genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. [electronic resource] by Freund, C L Gregory-Evans, C Y Furukawa, T Papaioannou, M Looser, J Ploder, L Bellingham, J Ng, D Herbrick, J A Duncan, A Scherer, S W Tsui, L C Loutradis-Anagnostou, A Jacobson, S G Cepko, C L Bhattacharya, S S McInnes, R R Producer: 19971223 In: Cell vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)